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Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant
- Dr J R Vermeesch, Center for Human Genetics, Herestraat 49, 3000 Leuven, Belgium; joris.vermeesch{at}uz.kuleuven.ac.be
Citation
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant
Publication history
- Received October 5, 2007
- Revised December 28, 2007
- Accepted January 7, 2008
- First published June 11, 2008.
Online issue publication
July 30, 2016
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- Previous version (27 April 2016).
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© Hannes et al 2009 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.